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再刊:不吸烟者中的肺癌。在分子诊断和靶向治疗时代,吸烟史是否重要?

Republished: lung cancer in never-smokers. Does smoking history matter in the era of molecular diagnostics and targeted therapy?

出版信息

Postgrad Med J. 2014 Apr;90(1062):228-35. doi: 10.1136/postgradmedj-2012-201296rep.

Abstract

Lung cancer in never-smokers was recognised as a distinct clinical entity around the mid-2000s because these patients tended to be Asian women and diagnosed at a younger age with a preponderance of adenocarcinoma and better survival outcome despite a more advanced stage of presentation. It was soon discovered that lung cancer in never-smokers had a higher prevalence of activating EGFR mutations and we tend to classify lung cancer by smoking status for screening purpose. With the discoveries of many actionable driver mutations such as activating EGFR mutations and ALK rearrangement in adenocarcinoma of the lung we have switched to classifying non-small cell lung cancer into different individual molecular subgroups based on the presence of a dominant driver mutation. Although many actionable driver mutations are found in never-smokers with adenocarcinoma, this review will summarise that a substantial proportion of patients with these actionable driver mutations had a previous smoking history. Alternatively among the driver mutations that are associated with smoking history, a fair amount of these patients were never-smokers. Thus smoking status should not be used as a screen strategy for identifying driver mutations in clinical practice. Finally smoking history may have predictive and/or prognostic significance within individual molecular subgroups and identifying the difference according to smoking history may help optimise future targeted therapy.

摘要

在 21 世纪中期,人们认识到从不吸烟的肺癌患者是一种独特的临床实体,因为这些患者往往是亚洲女性,且发病年龄较小,腺癌居多,尽管分期较晚,但生存预后较好。很快人们发现从不吸烟的肺癌患者 EGFR 激活突变的发生率更高,因此我们倾向于根据吸烟状态对肺癌进行分类,以便进行筛查。随着对许多可治疗驱动基因突变(如腺癌中的 EGFR 激活突变和 ALK 重排)的发现,我们已将非小细胞肺癌基于主要驱动基因突变的存在,分类为不同的分子亚型。尽管从不吸烟的腺癌患者中发现了许多可治疗的驱动基因突变,但本综述将总结出相当一部分具有这些可治疗驱动基因突变的患者有吸烟史。或者,在与吸烟史相关的驱动基因突变中,相当一部分患者从不吸烟。因此,在临床实践中,不应将吸烟状态作为识别驱动基因突变的筛查策略。最后,吸烟史可能在各个分子亚型中具有预测和/或预后意义,根据吸烟史进行区分可能有助于优化未来的靶向治疗。

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